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Nortriptyline Hydrochloride
Nortriptyline Hydrochloride - 68788-9749-6 - (Nortriptyline Hydrochloride)
Drug Information of Nortriptyline Hydrochloride
| Product NDC: | 68788-9749 |
| Proprietary Name: | Nortriptyline Hydrochloride |
| Non Proprietary Name: | Nortriptyline Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Nortriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nortriptyline Hydrochloride
| Product NDC: | 68788-9749 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074132 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of Nortriptyline Hydrochloride
| Package NDC: | 68788-9749-6 |
| Package Description: | 60 CAPSULE in 1 BOTTLE (68788-9749-6) |
NDC Information of Nortriptyline Hydrochloride
| NDC Code | 68788-9749-6 |
| Proprietary Name | Nortriptyline Hydrochloride |
| Package Description | 60 CAPSULE in 1 BOTTLE (68788-9749-6) |
| Product NDC | 68788-9749 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nortriptyline Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120305 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
